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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339285Erstellt: 24. Oktober 2026

Nicotinic Acid → Tert-butyl 2-(nicotinamido)ethylcarbamate

https://huagongshe.com/de/reaction/339285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNicotinic AcidHCID 938—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
EduktN-BOC-ethylenediamineHCID 187201—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 2-(nicotinamido)ethylcarbamateHCID 4745332874%

Reaktionsschritte

In a typical run, nicotinic acid (2.0 g, 16.2 mmol) was taken up in CH2Cl2 (20 mL) along with oxalyl chloride (1.4 mL, 16.2 mmol). After a few drops of DMF were added, the reaction mixture was stirred at room temperature until all the solids had dissolved and all gas evolution had ceased (1 h). This freshly prepared solution of the acid chloride was added dropwise at 0° C. to a solution containing tert-butyl 2-amino-ethylcarbamate (2.6 g, 16.2 mmol) and Et3N (3.4 mL, 24.2 mmol) in CH2Cl2 (200 mL). The resulting reaction mixture was warmed to room temperature and stirred for 2 h. It was then washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by silica gel chromatography (CH2Cl2) afforded tert-butyl 2-(nicotinamido)ethylcarbamate (3.1 g, 74%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045261E1
Quelldatensatzuspto-grants-2014_11
ORD IDord-dc789adbac8a4541a0339b20c141af4b
Quellennotizuspto-grants-2014_11